FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PULSONIC DIGITAL BLOOD PRESSURE MONITOR MODEL BP-3

K Number: K860287 · Decision Apr 28, 1986
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
9
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PULSONIC DIGITAL BLOOD PRESSURE MONITOR MODEL BP-3
K Number
K860287
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Healthcheck Corp.
Date Received
January 28, 1986
Decision Date
April 28, 1986
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXN), ordered by most recent decision date.

View all

Other Clearances by Healthcheck Corp.

K Number Device Name
K884489 C&T PREGNANCY TEST KIT
K874818 TENSTAR
K881003 DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1
K863181 HEALTHCHECK THERM-STRIP
K861946 PTK PLUS. HOME PREGNANCY TEST
K851379 HEALTHCHECK DIGITAL THERMOMETER MODEL 1 TH-2
K850070 HEALTHCHECK AUTO INFLATE DIGITAL BP MONITOR BP-2
K844281 PTK HEALTHCHECK PREGNANCY TEST KIT